scholarly journals Juvenile ossifying fibroma (JOF) – A rare case report

2021 ◽  
Vol 8 (1) ◽  
pp. 098-102
Author(s):  
Santosh Kumar Kumhar ◽  
Gaurav Mittal ◽  
Anmol Agarwal ◽  
Akash Bhatt

Juvenile ossifying fibroma (JOF) is a rare, benign, bone forming lesion of children and adolescents. When sited in the jaws, it is considered as an aggressive form of ossifying fibroma presenting with a wide range of clinical symptoms and a high incidence of recurrence. Although early detection and management is thought to eradicate it completely. The present case report focuses on the surgical yet conservative management of JOF in a 5 years old boy who reported with a year-long, progressive swelling on the left side of his face. The tumour was excised with minimal surgical intervention into a clearly defined and lobulated single mass using maxillary vestibular incision under general anaesthesia. The postoperative course was uneventful, and no signs of recurrence were found in the next 6 months follow-up period.

2016 ◽  
Vol 6 (1) ◽  
pp. 45-51
Author(s):  
Deepa Das Achath ◽  
Abhishek Sanjay Ghule ◽  
Preeti Kanchan-Talreja ◽  
Sunanda Bhatnagar

ABSTRACT Fibroosseous lesions of the jaws, including juvenile ossifying fibroma (JOF), pose diagnostic and therapeutic difficulties due to their clinical, radiological, and histological variability. There are two histological varieties of it, one as psammomatoid type and second as trebacular type; here, we present a trebacular type, which is a rare variety. After the clinical examination, radiological and histological analysis, it was diagnosed as juvenile trebacular ossifying fibroma. Although JOF is an uncommon clinical entity, its aggressive local behavior and high recurrence rate means that it is important to make an early diagnosis, apply the appropriate treatment, and, especially, follow-up the patient over the long term. How to cite this article Ghule AS, Achath DD, Kanchan- Talreja P, Bhatnagar S. Juvenile Aggressive Trabecular Ossifying Fibroma of Mandible: A Rare Case Report. J Contemp Dent 2016;6(1):45-51.


2017 ◽  
Vol 5 (6) ◽  
pp. 816-821 ◽  
Author(s):  
Lipsa Bhuyan ◽  
Abikshyeet Panda ◽  
Kailash Chandra Dash ◽  
Mohiddin S. Gouse ◽  
Kiran Misra

Author(s):  
MARA LUANA BATISTA SEVERO ◽  
THALITA SANTANA CONCEIÇÃO ◽  
EIDER GUIMARÃES BASTOS ◽  
ANDRÉ LUIS COSTA CANTANHEDE ◽  
FABIO LAGO ◽  
...  

2019 ◽  
Vol 3 ◽  
pp. 20-20
Author(s):  
Barakat Adeola Animasahun ◽  
Gbenga Kayode-Awe ◽  
Olusola Yejide Kusimo

10.3823/2621 ◽  
2020 ◽  
Vol 13 ◽  
Author(s):  
Glaucia Suzanna Jong-A-Liem ◽  
Bruno Vilhena Nascimento ◽  
Carlos Dos Reis Lisboa-Neto ◽  
Joel Monteiro de Jesus ◽  
Edson Bor-Seng-Shu ◽  
...  

Psammomatoid Juvenile Ossifying Fibroma is an uncommon fibro-osseous neoplasm of aggressive but benign nature found in the younger age. Its aggressive path can lead to facial deformation, eye proptosis, and development of intracranial extensions leading to various neurological symptoms. A systematic review based by the MOOSE guideline in Medline, EMBASE and Lilacs, resulted in 23 reported cases of intracranial extended PJOF. Hence, we found it relevant to present a case report of a 15-year-old male with facial deformation and left eye proptosis absent of visual disturbances with PJOF. The lesion was present in the left anterior base of the skull and extended to the intra-orbital space and over the zygomatic arch. The diagnosis was only confirmed as PJOF by histopathological analysis of the completely resected lesion. Follow up visits documented unremarkable regression of the facial deformity and post-op images showed a completely resected lesion. Our case raises the need to be aware of this rare tumor that can be confused with a meningioma or other intracranial tumors.


2014 ◽  
Vol 3 (54) ◽  
pp. 12517-12522
Author(s):  
Ranjit S Mandwe ◽  
Swapna Puri ◽  
Vivek Kolhe ◽  
Shrikant Shingne

Author(s):  
CARLA SAMILY DE OLIVEIRA COSTA ◽  
HELLEN BANDEIRA DE PONTES SANTOS ◽  
LARISSA SANTOS AMARAL ROLIM ◽  
RODRIGO PORPINO MAFRA ◽  
PATRÍCIA DAVIN GOMES PARENTE ◽  
...  

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